Infosys Limited
Senior Principal Consultant, Life sciences - Business Consulting
Infosys Limited, Dallas, Texas, United States, 75215
Senior Principal – Research and Development, Life Sciences
Apply fast, check the full description by scrolling below to find out the full requirements for this role. Infosys Consulting is seeking talented and motivated consultants to join our Life Sciences practice, focusing on Regulatory Sub Practice of Larger Life Sciences Consulting. RESPONSIBILITIES Deep knowledge of Pharma Regulatory Operations and Regulatory IT Systems, aligned with core Functional and Technical competencies. Expertise in Regulatory areas with the ability to drive innovative IT solutions, client engagement, and thought leadership. Understanding of processes related to health authority submissions, content authoring, labeling, lifecycle management of CMC, regulatory intelligence, and country-specific requirements. Strategize and advise on product roadmaps, working closely with clients to deliver solutions. Mentor and guide teams for positive outcomes. Lead strategic programs, manage planning, execution, reporting, resources, quality, stakeholder communication, client relationships, risks, mitigations, and budgets. Participate in sales pursuits, proposal development, and client presentations. Develop digital solutions for Life Sciences organizations, participate in industry engagements, and publish thought leadership. Contribute to practice development, coach junior staff, and participate in training. Travel up to 4 days a week to client sites. BASIC QUALIFICATIONS Combination of industry domain, process, technical, and consulting skills, including client management and executive communication. Master’s degree in Life Science, Medical, or related fields; MBA is a plus. 12-15 years of experience in Regulatory Strategy, Operations, and Intelligence in Biopharma and Medical Devices. Knowledge of RIM systems like Veeva Vault, LIQUENT, and publishing tools. Experience with regulatory IT systems, including integration and migration. Forward-thinking in patient support and market access strategies. Thought leadership and problem-solving skills. Authorized to work in the US without employer-sponsored visa; no immigration sponsorship provided. Estimated annual compensation for NY, NJ, and TX: $157,500 - $192,500. Benefits include health insurance, disability coverage, reimbursement accounts, insurance plans, 401(k), paid holidays, and PTO. About Us Infosys Consulting is a global management and technology consulting practice, enabling digital transformation through innovative strategies and solutions. We offer a collaborative environment, opportunities for impact, and a global culture. We are committed to equal employment opportunities regardless of race, gender, or other protected characteristics.
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Apply fast, check the full description by scrolling below to find out the full requirements for this role. Infosys Consulting is seeking talented and motivated consultants to join our Life Sciences practice, focusing on Regulatory Sub Practice of Larger Life Sciences Consulting. RESPONSIBILITIES Deep knowledge of Pharma Regulatory Operations and Regulatory IT Systems, aligned with core Functional and Technical competencies. Expertise in Regulatory areas with the ability to drive innovative IT solutions, client engagement, and thought leadership. Understanding of processes related to health authority submissions, content authoring, labeling, lifecycle management of CMC, regulatory intelligence, and country-specific requirements. Strategize and advise on product roadmaps, working closely with clients to deliver solutions. Mentor and guide teams for positive outcomes. Lead strategic programs, manage planning, execution, reporting, resources, quality, stakeholder communication, client relationships, risks, mitigations, and budgets. Participate in sales pursuits, proposal development, and client presentations. Develop digital solutions for Life Sciences organizations, participate in industry engagements, and publish thought leadership. Contribute to practice development, coach junior staff, and participate in training. Travel up to 4 days a week to client sites. BASIC QUALIFICATIONS Combination of industry domain, process, technical, and consulting skills, including client management and executive communication. Master’s degree in Life Science, Medical, or related fields; MBA is a plus. 12-15 years of experience in Regulatory Strategy, Operations, and Intelligence in Biopharma and Medical Devices. Knowledge of RIM systems like Veeva Vault, LIQUENT, and publishing tools. Experience with regulatory IT systems, including integration and migration. Forward-thinking in patient support and market access strategies. Thought leadership and problem-solving skills. Authorized to work in the US without employer-sponsored visa; no immigration sponsorship provided. Estimated annual compensation for NY, NJ, and TX: $157,500 - $192,500. Benefits include health insurance, disability coverage, reimbursement accounts, insurance plans, 401(k), paid holidays, and PTO. About Us Infosys Consulting is a global management and technology consulting practice, enabling digital transformation through innovative strategies and solutions. We offer a collaborative environment, opportunities for impact, and a global culture. We are committed to equal employment opportunities regardless of race, gender, or other protected characteristics.
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